Trafficking-deficient long QT syndrome mutation KCNQ1-T587M confers severe clinical phenotype by impairment of KCNH2 membrane localization: evidence for clinically significant IKr-IKs alpha-subunit interaction.
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| Description | scientific article |
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author: Flavien Charpentier Isabelle Baró Stanley Nattel Ralf P. Brandes Stefan H Hohnloser |
| Publication date | August 13, 2009 |
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